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Hydrodeoxygenation of Xylose Isopropylidene Ketal Over Pd/HBEA Catalyst for the Production of Green Fuels.
Souza, Matheus O; Pereira, Sergio C; Lau, Lam Y; Soter, Leandro; Pereira, Marcelo M.
Afiliação
  • Souza MO; Instituto de Química, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Pereira SC; Instituto de Química, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Lau LY; Instituto de Química, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Soter L; Instituto de Química, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Pereira MM; Instituto de Química, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Front Chem ; 9: 729787, 2021.
Article em En | MEDLINE | ID: mdl-34490211
1,2:3,5-Di-O-isopropylidene-α-D-xylofuranose (DX) is a major component of a new bio-crude: a viscous oil presenting petroleum-friendly properties produced by the ketalization of sugarcane bagasse. This article studies DX HDO (hydrodeoxygenation) over a Pd/HBEA catalyst in a batch reactor at 250°C. The effects of hydrogen pressure from 10 to 40 bar, catalyst/DX ratio from ½ to 2, and reaction time 0-24 h were investigated. A range of conditions for complete hydrodeoxygenated DX into alkanes with a Pd/HBEA catalyst was found. In these conditions, a low coke yield with water as the principal deoxygenated product was obtained. Further, higher amounts of alkanes containing seven or more carbons (A7+) were favored at 30 bar of hydrogen pressure, Cat/DX ratio = 2, and short reaction time. Products analysis that accompanied the above variations during reaction time led to general insights into reaction pathways. First, in the presence of DX, an effective n-hexane conversion was not observed on experiments of low catalyst/DX ratio (½) or in the initial period of high Cat/DX ratio, suggesting DX is much more successful than n-hexane to compete for active sites. Then, the formation of a pool of oxygenated compounds, such as furans, ketones, and carboxylic acids, along with lighter and heavier alkanes was observed. Hence, the aforementioned oxygenates may undergo reactions, such as aldol condensation with subsequent hydrodeoxygenation reaction, generating heavier alkanes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Chem Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Brasil País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Chem Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Brasil País de publicação: Suíça